Senior Drug Safety Associate (SA Based-US EST Hours)
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About the role
College degree in scientific/medical discipline, 5+ years drug safety/pharmacovigilance experience, MedDRA and WHO drug dictionary coding expertise, MS Office proficiency, knowledge of PV regulations and clinical trials.Key Responsibilitiesprocessing casesleading projectswriting narrativesSkills & ToolsMedDRA, WHO Drug Dictionary, Microsoft OfficeJob DetailsCategory: Research and Development (R&D)Seniority: Senior LevelCommitment: Full TimeWorkplace: Remote Bloemfontein or Johannesburg or Pretoria or Cape Town or DurbanLanguages: EnglishAbout MMSA global data-focused clinical research organization providing clinical research, regulatory, and health data solutions for pharmaceutical and biotech clients. Industry: Research and Development Apply To this Job .
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